Canonical Allele Identifier: PA2827468563
Gene: HPS4 HGNC NCBI
ClinVar RCV:
RCV000020872
ClinVar Variation:
21678
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336831.1:p.His154Arg
CA342358
NM_001349902.1:c.461A>G